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J Leisti

Showing results (1-10 of 89) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Clinical evaluation of congenital defects]J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Congenital defects as a clinical problem]J Leisti
Suomalainen Tiedeakatemia Toimituksia. Sar. A.4: Biologica|January 1, 1971
Structural variation in human nitotic chromosomesJ Leisti
Birth Defects Original Article Series|January 1, 1977
A case of deletion of short arm of chromosome 8J Leisti, P Aula
Human Genetics|September 12, 2000
An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish familyH Kokkonen, J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[From identification of mutation to population screening]P Aula, J Leisti
Clinical Genetics|November 1, 1980
Partial trisomy 1 (q42 leads to ter)J Leisti, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]H von Koskull, J Leisti
Human Genetics|May 1, 1995
A molecular and cytogenetic study in Finnish Prader-Willi patientsH Kokkonen, M Kähkönen, J Leisti
Journal of Medical Genetics|September 19, 2000
Epidemiology of neurofibromatosis type 1 (NF1) in northern FinlandM Poyhonen, S Kytölä, J Leisti
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Clinical evaluation of congenital defects]J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1981
[Congenital defects as a clinical problem]J Leisti
Suomalainen Tiedeakatemia Toimituksia. Sar. A.4: Biologica|January 1, 1971
Structural variation in human nitotic chromosomesJ Leisti
Birth Defects Original Article Series|January 1, 1977
A case of deletion of short arm of chromosome 8J Leisti, P Aula
Human Genetics|September 12, 2000
An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish familyH Kokkonen, J Leisti
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[From identification of mutation to population screening]P Aula, J Leisti
Clinical Genetics|November 1, 1980
Partial trisomy 1 (q42 leads to ter)J Leisti, P Aula
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]H von Koskull, J Leisti
Human Genetics|May 1, 1995
A molecular and cytogenetic study in Finnish Prader-Willi patientsH Kokkonen, M Kähkönen, J Leisti
Journal of Medical Genetics|September 19, 2000
Epidemiology of neurofibromatosis type 1 (NF1) in northern FinlandM Poyhonen, S Kytölä, J Leisti
Pageof 9